Evidence map›Paper›PMID 42728601›Full record

ArticleOrphanet journal of rare diseases2026

Diagnosis of rare diseases based on facial phenotype: a quantitative assessment using 2D and 3D photography in Stickler syndrome.

Adèle Rohée-Traoré, Maxime Taverne, Quentin Hennocq, Thomas Bongibault, Alejandra Daruich, Dominique Bremond-Gignac, Jean-Daniel Kün-Darbois, Pierre-Raphaël Rothschild, Roman-Hossein Khonsari

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Adèle Rohée-TraoréLaboratoire Forme et Croissance du Crâne, Institut Imagine, Paris, France. adele.rohee-traore@outlook.fr.ORCID http://orcid.org/0000-0002-6288-0491
Maxime TaverneLaboratoire Forme et Croissance du Crâne, Institut Imagine, Paris, France.
Quentin HennocqLaboratoire Forme et Croissance du Crâne, Institut Imagine, Paris, France.
Thomas BongibaultService de sciences des données, Institut Imagine, Paris, France.
Alejandra DaruichService d'ophtalmologie, Hôpital Necker - Enfants malades, Assistance Publique - Hôpitaux de Paris, Paris, France.
Dominique Bremond-GignacService d'ophtalmologie, Hôpital Necker - Enfants malades, Assistance Publique - Hôpitaux de Paris, Paris, France.
Jean-Daniel Kün-DarboisService de chirurgie maxillo-faciale, Centre Hospitalier Universitaire d'Angers, Angers, France.
Pierre-Raphaël RothschildService d'ophtalmologie - OphtalmoPôle de Paris, Hôpital Cochin - Port Royal, Assistance Publique - Hôpitaux de Paris, Paris, France.
Roman-Hossein KhonsariLaboratoire Forme et Croissance du Crâne, Institut Imagine, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stickler syndrome (SS) is a rare genetic disorder caused by mutations in collagen-encoding genes. Patients with SS are at an increased risk of retinal detachment, with ophthalmologic complications often presenting as the first symptom due to significant diagnostic delays. These delays contribute to severe visual impairment, even in early childhood, making diagnostic uncertainty a major clinical challenge. This study assessed the feasibility of early SS detection using facial features. Supervised machine learning models, including XGBoost and support vector machines (SVM), were applied to 2D and 3D facial photographs to differentiate individuals with SS from healthy controls. The models achieved 92% accuracy in identifying SS patients using full-face 2D and 3D photographs. When focusing specifically on the orbitonasal region in 3D images, classification accuracy increased to 96%. Facial morphology in rare diseases such as Stickler syndrome can serve as a highly accurate, non-invasive screening tool. AI-based analysis has the potential to reduce diagnostic delays and prevent associated complications, improving patient outcomes.

Indexed as

ArthritisConnective Tissue DiseasesHearing Loss, SensorineuralPhotographyRare DiseasesRetinal DetachmentChildFaceFemaleHumansMachine LearningMalePhenotypeArtificial intelligencePhotogrammetryPierre Robin syndromeRetinal detachmentStickler syndromeSupervised machine learning

Identifiers

PMID42728601
PMCPMC13570527

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.